M. Parera

In hereditary hemochromatosis, red cell apheresis removes excess iron twice as fast as manual whole blood phlebotomy

J. Besalduch, J. Muncunill, A. Obrador, 2002, Journal of clinical apheresis.

Prevalence of HFE C282Y and H63D in Jewish populations and clinical implications of H63D homozygosity

A. Picornell, A. Obrador, M. Matas, 2006, Clinical genetics.

Prevalence of the C282Y mutation for haemochromatosis on the Island of Majorca

J. Rossell, A. Picornell, C. Tomàs, 2000, Clinical genetics.

Balearic archipelago: three islands, three beta‐thalassemia population patterns

A. Picornell, H. López-Escribano, M. Parera, 2013, Clinical genetics.

Distribution of HFE C282Y and H63D mutations in the Balearic Islands (NE Spain)

A. Picornell, A. Obrador, A. Galmés, 2002, Clinical genetics.